| Primary Device ID | 50085412677786 |
| NIH Device Record Key | b79e88c8-49b1-41f6-8892-2e5e083f19d9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CLEARLINK/DUO-VENT |
| Version Model Number | 2R8420 |
| Catalog Number | 2R8420 |
| Company DUNS | 005083209 |
| Company Name | BAXTER HEALTHCARE CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| medinfo_medproducts@baxter.com |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Length | 120 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00085412677781 [Primary] |
| GS1 | 50085412677786 [Package] Contains: 00085412677781 Package: CASE [48 Units] In Commercial Distribution |
| FPA | Set, administration, intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-03 |
| Device Publish Date | 2025-01-24 |
| 50085412677786 | Non-DEHP Solution Set with DUO-VENT Spike, Luer Activated Valve, Male Luer Lock Adapter with Ret |
| 50085412677762 | Non-DEHP Solution Set with DUO-VENT Spike, Luer Activated Valve, Male Luer Lock Adapter with Ret |